A Phase I Study to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics of GSK2118436 in Subjects With Solid Tumors

Exclusion Criteria

• •Currently receiving cancer therapy (chemotherapy, radiation therapy, immuno-therapy, biologic therapy, hormonal therapy, surgery and/or tumor embolization).
• •Use of an investigational anti-cancer drug within 28 days preceding the first dose of GSK2118436.
• •Current use of a prohibited medication as defined in the protocol or requires any of these medications during treatment with GSK2118436.
• •Current use of therapeutic warfarin.
• •Any major surgery, radiotherapy, or immunotherapy within 4 weeks prior to first dose. Limited radiotherapy within 2 weeks prior to first dose.
• •Chemotherapy regimens with delayed toxicity within four weeks prior to first dose (6 weeks for prior nitrosourea or mitomycin C). Chemotherapy regimens given continuously or on a weekly basis with limited potential for delayed toxicity within 2 weeks prior to first dose.
• •Unresolved toxicity greater than National Cancer Institute Common Terminology Criteria for Adverse Events, version 3.0 Grade 1 from previous anti-cancer therapy except alopecia unless agreed to by a GSK Medical Monitor and the investigator.
• •Presence of active gastrointestinal disease or other condition that will interfere significantly with the absorption, distribution, metabolism, or excretion of drugs.
• •A history of known HIV infection.
• •Primary malignancy of the central nervous system.
• •Symptomatic or untreated leptomeningeal or brain metastases or spinal cord compression. Subjects previously treated for these conditions that are asymptomatic and off corticosteroids for at least two weeks are permitted. Brain metastases must be stable for at least 3 months with verification by imaging (brain MRI completed at screening). Subjects are not permitted to receive enzyme inducing anti-epileptic drugs (EIAEDs). In Part 2 of the study, subjects with asymptomatic, untreated brain metastases that have not been stable for 3 months may be enrolled with approval of the GSK medical monitor. These subjects can be on a stable dose of corticosteroids.
• •History of alcohol or drug abuse within 6 months prior to the screen visit.
• •Psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol.
• •Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol.
• •QTc interval greater than or equal to 480 msecs.
• •History of acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting within 24 weeks prior to the first dose.
• •Class II, III, or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.
• •Abnormal cardiac valve morphology (subjects with minimally abnormalities can be entered on study with approval from the GSK medical monitor).
• •Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drug, or excipients as described in the protocol (to date there are no known FDA approved drugs chemically related to GSK2118436).
• •Pregnant or lactating female.
• •Unwillingness or inability to follow the procedures outlined in the protocol.
• •Subjects with known glucose 6 phosphate dehydrogenase (G6PD) deficiency.
• •Patients positive for HPV. Entry on study allowed only at the discretion of subject and investigator after informed consent regarding discussion of the risk of papillomavirus infection. If enrolled, these subjects must use condoms for sexual activity, regardless of the use of other contraceptive measures and childbearing status.
• •Prior treatment with a BRAF or MEK inhibitor unless approved by the GSK medical monitor.